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Journal articles on the topic 'Genes, Immediate-Early'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 January 2023

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1

Polyakov, P. P., A. S. Lipatova, and A. H. Kade. "MECHANISMS OF IMMEDIATE-EARLY GENES ACTIVATION." Medical Herald of the South of Russia, no. 4 (January 1, 2016): 4–11. http://dx.doi.org/10.21886/2219-8075-2016-4-4-11.

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2

Bullitt, Elizabeth. "Immediate-early genes and chronic pain." APS Journal 3, no. 1 (March 1994): 53–55. http://dx.doi.org/10.1016/s1058-9139(05)80236-0.

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3

Chiasson, Bernard J., Zoe Dennison, and Harold A. Robertson. "Amygdala kindling and immediate-early genes." Molecular Brain Research 29, no. 1 (March 1995): 191–99. http://dx.doi.org/10.1016/0169-328x(94)00250-i.

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4

Morgan, James I., and Tom Curran. "Immediate-early genes: ten years on." Trends in Neurosciences 18, no. 2 (February 1995): 66–67. http://dx.doi.org/10.1016/0166-2236(95)80022-t.

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5

Lanahan, Anthony, and Paul Worley. "Immediate-Early Genes and Synaptic Function." Neurobiology of Learning and Memory 70, no. 1-2 (July 1998): 37–43. http://dx.doi.org/10.1006/nlme.1998.3836.

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6

SCHILLING, KARL, TOM CURRAN, and JAMES I. MORGAN. "Fosvergnügen The Excitement of Immediate-Early Genes." Annals of the New York Academy of Sciences 627, no. 1 (August 1991): 115–23. http://dx.doi.org/10.1111/j.1749-6632.1991.tb25917.x.

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7

Robertson, H. A. "Immediate-early genes, neuronal plasticity, and memory." Biochemistry and Cell Biology 70, no. 9 (September 1, 1992): 729–37. http://dx.doi.org/10.1139/o92-112.

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The demonstration that the immediate-early gene c-fos is rapidly and transiently expressed in brain following a variety of manipulations has led to intense study of these genes to determine what physiological role they play. The very wide range of stimuli which lead to induction of immediate-early genes (IEGs) in the brain has raised concerns for the specificity of their actions and the suggestion that they might merely be involved in housekeeping functions. On the other hand, there is evidence that these genes may play a role in the transmission of information from cell surface receptors to the genetic material in many instances of neuronal plasticity, including development of seizure susceptibility (kindling), long-term potentiation, drug-induced changes, the phase shift in circadian rhythms, and spreading neuronal depression. In addition to being a putative third (or fourth) messenger involved in transduction of signals to the genetic material, activation of IEGs has proven to be a useful tool for the study of transsynaptic activation of certain neuronal pathways in the brain. Thus, studies on the induction of IEGs are proving to be especially useful in understanding some important functions and properties of the mammalian brain.Key words: immediate-early genes, brain, memory, neuronal plasticity, gene expression.

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8

Healy, Shannon, Protiti Khan, and James R. Davie. "Immediate early response genes and cell transformation." Pharmacology & Therapeutics 137, no. 1 (January 2013): 64–77. http://dx.doi.org/10.1016/j.pharmthera.2012.09.001.

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9

Iadarola, Michael J. "Stimulus-transcription coupling and immediate-early genes." APS Journal 3, no. 1 (March 1994): 56–59. http://dx.doi.org/10.1016/s1058-9139(05)80237-2.

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10

Kawasaki, Takeru, Masahiro Tanaka, Makoto Fujie, Shoji Usami, and Takashi Yamada. "Immediate early genes expressed in chlorovirus infections." Virology 318, no. 1 (January 2004): 214–23. http://dx.doi.org/10.1016/j.virol.2003.09.015.

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11

Roche, E., and M. Prentki. "Calcium regulation of immediate-early response genes." Cell Calcium 16, no. 4 (October 1994): 331–38. http://dx.doi.org/10.1016/0143-4160(94)90097-3.

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12

Minson, J. B., L. F. Arnolda, I. J. Llewellyn-Smith, P. M. Pilowsky, S. Suzuki, and J. P. Chalmers. "Immediate Early Genes in Blood Pressure Regulation." Clinical and Experimental Hypertension 18, no. 3-4 (January 1996): 279–90. http://dx.doi.org/10.3109/10641969609088963.

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13

Gladbach, Amadeus, Yazi Ke, Arne Ittner, and Lars Ittner. "P3-015: Tau-dependent immediate early genes." Alzheimer's & Dementia 8, no. 4S_Part_12 (July 2012): P460. http://dx.doi.org/10.1016/j.jalz.2012.05.1233.

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14

Kornhauser, Jon M., Kelly E. Mayo, and Joseph S. Takahashi. "Light, immediate-early genes, and circadian rhythms." Behavior Genetics 26, no. 3 (May 1996): 221–40. http://dx.doi.org/10.1007/bf02359382.

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15

Beadling, C., K. W. Johnson, and K. A. Smith. "Isolation of interleukin 2-induced immediate-early genes." Proceedings of the National Academy of Sciences 90, no. 7 (April 1, 1993): 2719–23. http://dx.doi.org/10.1073/pnas.90.7.2719.

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16

Worley, P. F., A. J. Cole, T. H. Murphy, B. A. Christy, Y. Nakabeppu, and J. M. Baraban. "Synaptic Regulation of Immediate-Early Genes in Brain." Cold Spring Harbor Symposia on Quantitative Biology 55 (January 1, 1990): 213–23. http://dx.doi.org/10.1101/sqb.1990.055.01.023.

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17

Schreiber, Steven S., Georges Tocco, Tracey J. Shors, and Richard F. Thompson. "Activation of immediate early genes after acute stress." NeuroReport 2, no. 1 (January 1991): 17–20. http://dx.doi.org/10.1097/00001756-199101000-00004.

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18

Dragunow, M., R. W. Currie, R. L. M. Faull, H. A. Robertson, and K. Jansen. "Immediate-early genes, kindling and long-term potentiation." Neuroscience & Biobehavioral Reviews 13, no. 4 (December 1989): 301–13. http://dx.doi.org/10.1016/s0149-7634(89)80066-1.

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19

Tischmeyer, W., and R. Grimm. "Activation of immediate early genes and memory formation." Cellular and Molecular Life Sciences (CMLS) 55, no. 4 (April 1, 1999): 564–74. http://dx.doi.org/10.1007/s000180050315.

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20

Robertson, H. A. "Immediate-early genes in the central nervous system." Journal of Chemical Neuroanatomy 11, no. 2 (August 1996): 144. http://dx.doi.org/10.1016/0891-0618(96)81572-9.

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21

Khachigian, Levon. "Immediate-early genes as master switches in disease." Cell Biology International 32, no. 3 (March 2008): S3. http://dx.doi.org/10.1016/j.cellbi.2008.01.018.

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22

KAUFMAN, GALEN D. "Activation of Immediate Early Genes by Vestibular Stimulation." Annals of the New York Academy of Sciences 781, no. 1 Lipids and Sy (June 1996): 437–42. http://dx.doi.org/10.1111/j.1749-6632.1996.tb15718.x.

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23

Doucet, John P., and Nicolas G. Bazan. "Excitable membranes, lipid messengers, and immediate-early genes." Molecular Neurobiology 6, no. 4 (December 1992): 407–24. http://dx.doi.org/10.1007/bf02757944.

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24

Morgan, J. I. "Immediate early genes: Functions and responses to drugs." European Neuropsychopharmacology 6 (September 1996): S4–27—S4–28. http://dx.doi.org/10.1016/0924-977x(96)82891-4.

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25

Kelly, K. "Immediate-early genes induced by antigen receptor stimulation." Current Opinion in Immunology 7, no. 3 (1995): 327–32. http://dx.doi.org/10.1016/0952-7915(95)80106-5.

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26

Lantz, Mikael, Tereza Vondrichova, Hemang Parikh, Christofer Frenander, Martin Ridderstråle, Peter Åsman, Magnus Åberg, Leif Groop, and Bengt Hallengren. "Overexpression of Immediate Early Genes in Active Graves’ Ophthalmopathy." Journal of Clinical Endocrinology & Metabolism 90, no. 8 (August 2005): 4784–91. http://dx.doi.org/10.1210/jc.2004-2275.

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27

Kubik, S., T. Miyashita, and J. F. Guzowski. "Using immediate-early genes to map hippocampal subregional functions." Learning & Memory 14, no. 11 (November 14, 2007): 758–70. http://dx.doi.org/10.1101/lm.698107.

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28

Bigsby, R. M., and A. Li. "Differentially regulated immediate early genes in the rat uterus." Endocrinology 134, no. 4 (April 1994): 1820–26. http://dx.doi.org/10.1210/endo.134.4.8137748.

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29

Schaukowitch, Katie, Jae-Yeol Joo, Xihui Liu, Jonathan K. Watts, Carlos Martinez, and Tae-Kyung Kim. "Enhancer RNA Facilitates NELF Release from Immediate Early Genes." Molecular Cell 56, no. 1 (October 2014): 29–42. http://dx.doi.org/10.1016/j.molcel.2014.08.023.

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30

Sauvage, Magdalena, Takashi Kitsukawa, and Erika Atucha. "Single-cell memory trace imaging with immediate-early genes." Journal of Neuroscience Methods 326 (October 2019): 108368. http://dx.doi.org/10.1016/j.jneumeth.2019.108368.

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31

Sheng, Hui Z., Peng X. Lin, and Phillip G. Nelson. "Combinatorial expression of immediate early genes in single neurons." Molecular Brain Research 30, no. 2 (June 1995): 196–202. http://dx.doi.org/10.1016/0169-328x(94)00291-l.

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32

Kawasaki, T., K. Nishida, M. Fujie, S. Usami, and T. Yamada. "Characterization of immediate early genes expressed in chlorovirus infection." Nucleic Acids Symposium Series 44, no. 1 (October 1, 2000): 161–62. http://dx.doi.org/10.1093/nass/44.1.161.

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33

Hunt, G. E., and I. S. McGregor. "Induction of immediate early genes following rewarding brain stimulation." European Neuropsychopharmacology 6 (June 1996): 120. http://dx.doi.org/10.1016/0924-977x(96)87859-x.

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34

Nakazawa, Kazutoshi, Laddawan Karachot, and Tetsuo Yamamori. "Differential expression of immediate early genes in cerebellar slices." Neuroscience Research Supplements 17 (January 1992): 71. http://dx.doi.org/10.1016/0921-8696(92)90744-l.

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35

Packham, Graham, Matthew Brimmell, David Cook, Alison J. Sinclair, and Paul J. Farrell. "Strain Variation in Epstein-Barr Virus Immediate Early Genes." Virology 192, no. 2 (February 1993): 541–50. http://dx.doi.org/10.1006/viro.1993.1070.

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36

Tang, Ruizhe, Liqun Lu, Beiyang Wang, Jiao Yu, and Hao Wang. "Identification of the Immediate-Early Genes of Cyprinid Herpesvirus 2." Viruses 12, no. 9 (September 7, 2020): 994. http://dx.doi.org/10.3390/v12090994.

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Cyprinid herpesvirus 2 (CyHV-2), which infects goldfish and crucian carp causing high mortality, is an emerging viral pathogen worldwide. The genome of CyHV-2 is large and comprises double-stranded DNA, including several genes similar to cyprinid herpesvirus 1, ictalurid herpesvirus-1, cyprinid herpesvirus 3, and ranid herpesvirus-1. Genes of DNA viruses are expressed in three temporal phases: immediate-early (IE), early (E), and late (L) genes. Viral IE genes initiate transcription as soon as the virus enters the host, without viral DNA replication. IE gene products enable the efficient expression of E and L genes or regulate the host to initiate virus replication. In the present study, five IE genes of CyHV-2 were identified, including open reading frame (ORF)54, ORF121, ORF141, ORF147, and ORF155. Time course analysis and reverse transcription polymerase chain reaction confirmed five IE genes, thirty-four E genes, and thirty-nine L genes. In addition, all 150 ORFs identified in the CyHV-2 genome are transcribed, and are expressed in chronological order, similar to other herpesviruses. This study is the first to identify the IE genes of CyHV-2, which will provide more information for viral molecular characterization.

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37

Lanahan, A., J. B. Williams, L. K. Sanders, and D. Nathans. "Growth factor-induced delayed early response genes." Molecular and Cellular Biology 12, no. 9 (September 1992): 3919–29. http://dx.doi.org/10.1128/mcb.12.9.3919-3929.1992.

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Growth factors induce the sequential expression of cellular genes whose products are thought to mediate long-term responses to the growth factors. In mouse 3T3 fibroblastic cells, the first genes to be expressed (immediate-early genes) are activated within minutes after the addition of platelet-derived growth factor, fibroblast growth factor, or serum. By cDNA cloning, we have identified genes that are activated after a delay of a few hours and several hours prior to serum-induced DNA replication. Activation of these delayed early response genes requires new protein synthesis, presumably the synthesis of immediate-early transcription factors described previously. Partial or complete sequencing of 13 different delayed early cDNAs, representing about 40% of the 650 primary cDNA isolates, revealed that 8 were related to known gene sequences and 5 were not. Among the former are cDNAs encoding nonhistone chromosomal proteins [HMGI(Y) and HMGI-C], adenine phosphoribosyltransferase (APRT), a protein related to human macrophage migration inhibitory factor (MIF), a protein of the major intrinsic protein (MIP) family homologous to the integral membrane protein of human erythrocytes, and cyclin CYL1. In 3T3 cells, the delayed early gene response to growth factors appears to be at least as complex as the immediate-early gene response previously described.

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38

Lanahan, A., J. B. Williams, L. K. Sanders, and D. Nathans. "Growth factor-induced delayed early response genes." Molecular and Cellular Biology 12, no. 9 (September 1992): 3919–29. http://dx.doi.org/10.1128/mcb.12.9.3919.

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Growth factors induce the sequential expression of cellular genes whose products are thought to mediate long-term responses to the growth factors. In mouse 3T3 fibroblastic cells, the first genes to be expressed (immediate-early genes) are activated within minutes after the addition of platelet-derived growth factor, fibroblast growth factor, or serum. By cDNA cloning, we have identified genes that are activated after a delay of a few hours and several hours prior to serum-induced DNA replication. Activation of these delayed early response genes requires new protein synthesis, presumably the synthesis of immediate-early transcription factors described previously. Partial or complete sequencing of 13 different delayed early cDNAs, representing about 40% of the 650 primary cDNA isolates, revealed that 8 were related to known gene sequences and 5 were not. Among the former are cDNAs encoding nonhistone chromosomal proteins [HMGI(Y) and HMGI-C], adenine phosphoribosyltransferase (APRT), a protein related to human macrophage migration inhibitory factor (MIF), a protein of the major intrinsic protein (MIP) family homologous to the integral membrane protein of human erythrocytes, and cyclin CYL1. In 3T3 cells, the delayed early gene response to growth factors appears to be at least as complex as the immediate-early gene response previously described.

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39

Mohn, K. L., T. M. Laz, J. C. Hsu, A. E. Melby, R. Bravo, and R. Taub. "The immediate-early growth response in regenerating liver and insulin-stimulated H-35 cells: comparison with serum-stimulated 3T3 cells and identification of 41 novel immediate-early genes." Molecular and Cellular Biology 11, no. 1 (January 1991): 381–90. http://dx.doi.org/10.1128/mcb.11.1.381-390.1991.

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Liver regeneration provides a unique system for analysis of mitogenesis in intact, fully developed animals. Cellular immediate-early genes likely play an important role in cell cycle regulation and have been extensively studied in mitogen-stimulated fibroblasts lymphocytes but not in liver. We have begun to characterize the immediate-early growth response genes of mitogen-stimulated liver cells, specifically, regenerating liver and insulin-stimulated Reuber H-35 hepatoma cells, and to address differences in growth response between different cell types. Through subtraction and differential screening of cDNA libraries from regenerating liver and insulin-treated H-35 cells, we have extensively characterized 341 differentially expressed clones and identified 52 immediate-early genes. These genes have been partially sequenced and subjected to Northern (RNA) blot analysis, and 41 appear to be novel. Surprisingly, two-thirds of these genes are also expressed in BALB/c 3T3 cells, but only 10 were identified in previous studies of 3T3 cells, and of these, 6 include well-known genes like jun and fos, and only 4 are novel. Approximately one-third of the immediate-early genes identified in mitogen-stimulated liver cells or serum-stimulated NIH 3T3 cells are expressed in a tissue-specific fashion, indicating that cell type-specific regulation of the proliferative response occurs during the immediate-early period. Our findings indicate that the immediate-early response is unusually complex for the first step in a regulatory cascade, suggesting that multiple pathways must be activated. The abundance of immediate-early genes and the highly varied pattern of their expression in different cell types suggest that the tissue specificity of the proliferative response arises from the particular set of these genes expressed in a given tissue.

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40

Mohn, K. L., T. M. Laz, J. C. Hsu, A. E. Melby, R. Bravo, and R. Taub. "The immediate-early growth response in regenerating liver and insulin-stimulated H-35 cells: comparison with serum-stimulated 3T3 cells and identification of 41 novel immediate-early genes." Molecular and Cellular Biology 11, no. 1 (January 1991): 381–90. http://dx.doi.org/10.1128/mcb.11.1.381.

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Abstract:

Liver regeneration provides a unique system for analysis of mitogenesis in intact, fully developed animals. Cellular immediate-early genes likely play an important role in cell cycle regulation and have been extensively studied in mitogen-stimulated fibroblasts lymphocytes but not in liver. We have begun to characterize the immediate-early growth response genes of mitogen-stimulated liver cells, specifically, regenerating liver and insulin-stimulated Reuber H-35 hepatoma cells, and to address differences in growth response between different cell types. Through subtraction and differential screening of cDNA libraries from regenerating liver and insulin-treated H-35 cells, we have extensively characterized 341 differentially expressed clones and identified 52 immediate-early genes. These genes have been partially sequenced and subjected to Northern (RNA) blot analysis, and 41 appear to be novel. Surprisingly, two-thirds of these genes are also expressed in BALB/c 3T3 cells, but only 10 were identified in previous studies of 3T3 cells, and of these, 6 include well-known genes like jun and fos, and only 4 are novel. Approximately one-third of the immediate-early genes identified in mitogen-stimulated liver cells or serum-stimulated NIH 3T3 cells are expressed in a tissue-specific fashion, indicating that cell type-specific regulation of the proliferative response occurs during the immediate-early period. Our findings indicate that the immediate-early response is unusually complex for the first step in a regulatory cascade, suggesting that multiple pathways must be activated. The abundance of immediate-early genes and the highly varied pattern of their expression in different cell types suggest that the tissue specificity of the proliferative response arises from the particular set of these genes expressed in a given tissue.

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41

Schmahl, Jennifer, Christopher S. Raymond, and Philippe Soriano. "PDGF signaling specificity is mediated through multiple immediate early genes." Nature Genetics 39, no. 1 (December 3, 2006): 52–60. http://dx.doi.org/10.1038/ng1922.

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42

Cobellis, Gilda, Caterina Missero, Barbara Simionati, Giorgio Valle, and Roberto Di Lauro. "Immediate early genes induced by H-Ras in thyroid cells." Oncogene 20, no. 18 (April 2001): 2281–90. http://dx.doi.org/10.1038/sj.onc.1204320.

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43

Lamprecht, Raphael, and Yadin Dudai. "Differential modulation of brain immediate early genes by intraperitoneal LiCI." NeuroReport 7, no. 1 (December 1995): 289–93. http://dx.doi.org/10.1097/00001756-199512000-00069.

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44

Lamprecht, Raphael, and Yadin Dudai. "Differential modulation of brain immediate early genes by intraperitoneal LiCl." NeuroReport 7, no. 1 (December 1995): 289–93. http://dx.doi.org/10.1097/00001756-199512290-00069.

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45

Basbaum, Allan. "Immediate-early genes and pain: What's all the “Fos” about?" APS Journal 3, no. 1 (March 1994): 49–52. http://dx.doi.org/10.1016/s1058-9139(05)80235-9.

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46

Aebert, Hermann, Torsten Cornelius, Tobias Ehr, Stephan R. Holmer, Dietrich E. Birnbaum, Günter A. J. Riegger, and Heribert Schunkert. "Expression of Immediate Early Genes After Cardioplegic Arrest and Reperfusion." Annals of Thoracic Surgery 63, no. 6 (June 1997): 1669–75. http://dx.doi.org/10.1016/s0003-4975(97)00272-5.

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47

Cho, Younsook, Tzy-Wen L. Gong, Ariane Kanicki, Richard A. Altschuler, and Margaret I. Lomax. "Noise overstimulation induces immediate early genes in the rat cochlea." Molecular Brain Research 130, no. 1-2 (November 2004): 134–48. http://dx.doi.org/10.1016/j.molbrainres.2004.07.017.

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48

Harlan, Richard E., and Meredith M. Garcia. "Drugs of abuse and immediate-early genes in the forebrain." Molecular Neurobiology 16, no. 3 (June 1998): 221–67. http://dx.doi.org/10.1007/bf02741385.

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49

Bing, Guoying, David Filer, Jeannette C. Miller, and Eric A. Stone. "Noradrenergic activation of immediate early genes in rat cerebral cortex." Molecular Brain Research 11, no. 1 (August 1991): 43–46. http://dx.doi.org/10.1016/0169-328x(91)90019-t.

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50

Ierusalimsky, Victor N., Matvey V. Roshchin, and Pavel M. Balaban. "Immediate-Early Genes Detection in the CNS of Terrestrial Snail." Cellular and Molecular Neurobiology 40, no. 8 (March 11, 2020): 1395–404. http://dx.doi.org/10.1007/s10571-020-00825-2.

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